Proton Rahman
Memorial University
154 Le Marchant Road
St. John's
Newfoundland A1C 5B8
Canada
Name/email consistency: high
- Genetics of Psoriasis and Psoriatic Arthritis: A Report from the GRAPPA 2010 Annual Meeting. Rahman, P., Elder, J.T. J. Rheumatol. (2012)
- Autosome-wide Copy Number Variation Association Analysis for Rheumatoid Arthritis Using the WTCCC High-density SNP Genotype Data. Uddin, M., Sturge, M., Rahman, P., Woods, M.O. J. Rheumatol. (2011)
- Association of interleukin 23 receptor variants with psoriatic arthritis. Rahman, P., Inman, R.D., Maksymowych, W.P., Reeve, J.P., Peddle, L., Gladman, D.D. J. Rheumatol. (2009)
- Psoriatic arthritis: genetic susceptibility and pharmacogenetics. Rahman, P., O'Rielly, D.D. Pharmacogenomics (2008)
- Association of interleukin-23 receptor variants with ankylosing spondylitis. Rahman, P., Inman, R.D., Gladman, D.D., Reeve, J.P., Peddle, L., Maksymowych, W.P. Arthritis Rheum. (2008)
- Genetics of ankylosing spondylitis: an update. Rahman, P. Curr. Rheumatol. Rep (2007)
- TNFalpha polymorphisms and risk of psoriatic arthritis. Rahman, P., Siannis, F., Butt, C., Farewell, V., Peddle, L., Pellett, F., Gladman, D. Ann. Rheum. Dis. (2006)
- Association between the interleukin-1 family gene cluster and psoriatic arthritis. Rahman, P., Sun, S., Peddle, L., Snelgrove, T., Melay, W., Greenwood, C., Gladman, D. Arthritis Rheum. (2006)
- Association of SEEK1 and psoriatic arthritis in two distinct Canadian populations. Rahman, P., Butt, C., Siannis, F., Farewell, V.T., Peddle, L., Pellett, F.J., Schentag, C., Gladman, D.D. Ann. Rheum. Dis. (2005)
- Genetic epidemiology of psoriasis and psoriatic arthritis. Rahman, P., Elder, J.T. Ann. Rheum. Dis. (2005)
- CARD15: a pleiotropic autoimmune gene that confers susceptibility to psoriatic arthritis. Rahman, P., Bartlett, S., Siannis, F., Pellett, F.J., Farewell, V.T., Peddle, L., Schentag, C.T., Alderdice, C.A., Hamilton, S., Khraishi, M., Tobin, Y., Hefferton, D., Gladman, D.D. Am. J. Hum. Genet. (2003)
- The Newfoundland population: a unique resource for genetic investigation of complex diseases. Rahman, P., Jones, A., Curtis, J., Bartlett, S., Peddle, L., Fernandez, B.A., Freimer, N.B. Hum. Mol. Genet. (2003)